MeSH Browser

MeSH Supplementary: Tyrosine Kinase 2 Deficiency
Unique ID: C566928
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566928
Entry Term(s): HIES with Atypical Mycobacteriosis, Autosomal Recessive; Hyper-IgE Syndrome with Atypical Mycobacteriosis, Autosomal Recessive; TYK2 Deficiency
Registry Numbers: 0
Heading Mapped to: *Job Syndrome; TYK2 Kinase / deficiency
Frequency: 9
Note: mutation in TYK2
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Tyrosine Kinase 2 Deficiency MeSH Supplementary Concept Data 2025